Clinical Document Specialist

☞ Covance

View: 109

Update day: 07-05-2024

Location: Leeds Yorkshire and the Humber

Category: Administrative / Clerical / Assistant

Industry: Staffing Recruiting Biotechnology Pharmaceuticals

Position: Entry level

Job type: Full-time

Loading ...

Job content

Job Overview

Your new employer is Labcorp Drug Development, the world’s most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

Labcorp Drug Development is seeking a Clinical Document Specialist to join the Clinical Pharmacology Services Team in Leeds, West Yorkshire. Your new position is a full-time and permanent position and you will play an integral role in supporting the Project Management team.

Your main responsibilities will include but not be restricted to:
  • Provides administrative support for effective study project teams within global Early Clinical Biometrics, including maintaining Biometric project files, eTMF/TMFs in accordance with relevant regulatory requirements.
  • May assist project teams in meeting minutes or action follow-ups.
  • Maintain the Biometric sections of eTMF tracker, working with Study Project Manager, study teams and applicable business partners for reconciliation of the files as part of the quality control process.
  • eTMF document upload.
  • Original document and/or binder management.
  • Original document packaging and archiving coordination with external off-site storage vendors.
  • Original document off-site storage retention tracking (US only).
  • Maintenance and organization of any on-site storage archive area or dedicated room.
  • Support of any eTMF configuration required for Biometrics.
  • Proactively maintains documents within the standardized filing structure for study documents.
  • Reports on non-compliance of document binder documents.
  • Performing documentation quality checks, identifying and following up on quality issues with relevant DM staff.
  • Training and supporting others in study filing, archiving and eTMF practices.
  • Assist department management team with maintaining tracking tools and metric data.
  • Gathering, organising, scanning and shipping of Biometrics project documentation as required.
  • Performs other duties as assigned by management to support study teams needing collaborative support.
Get ready to redefine what’s possible and discover your extraordinary potential at Labcorp Drug Development. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us as we speed the delivery of ground breaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients and your career.

Education/Qualifications
  • A minimum of 5 GCSEs A to C grade to include English, Science and Maths. A-levels preferred but not essential.

Experience
  • No prior experience necessary for role but administration skills would be advantageous.

Covance is proud to be an Equal Opportunity Employer:

 As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
Loading ...
Loading ...

Deadline: 21-06-2024

Click to apply for free candidate

Apply

Report job
Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...